A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170237



Internal ID21314298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:142202639..142207042hg38UCSC Ensembl
Outerchr5:142200306..142214063hg38UCSC Ensembl
Innerchr5:141582204..141586607hg19UCSC Ensembl
Outerchr5:141579871..141593628hg19UCSC Ensembl
Innerchr5:141562388..141566791hg18UCSC Ensembl
Outerchr5:141560055..141573812hg18UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3813758
hg1913758
hg1813758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14242603, nssv14245761, nssv14244297
SamplesNGO_19, NGO_26, NGO_15
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170237
Frequency
Sample Size93
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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